GENETIC ENCYCLOPEDIA
ABOUT US    

   

GRCh37/hg19 15q21.3-22.2(chr15:58088503-62221756)x1 AND See cases

Significance: Pathogenic
ClinVar: RCV000510898

Variant: GRCh37/hg19 15q21.3-22.2(chr15:58088503-62221756)x1

Type: Variant
Allele: GRCh37/hg19 15q21.3-22.2(chr15:58088503-62221756)x1 436298
Gene:
Type: copy number loss
Location: Chr15: 58088503 - 62221756 - assembly GRCh37
References: dbVar: nsv2774337
dbVar: nssv13655134

Condition

PhenotypeInstruction: See cases